The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
126101191 12610119 1 I 2016 20160728 20160801 20160801 EXP PHHY2016HR103775 NOVARTIS 0.00 M Y 0.00000 20160801 CN HR HR

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
126101191 12610119 1 PS TASIGNA NILOTINIB 1 Unknown 4X200 MG,PER DAY Y 22068 200 MG CAPSULE
126101191 12610119 2 SS TASIGNA NILOTINIB 1 Unknown 2X200 MG,PER DAY Y 22068 200 MG CAPSULE
126101191 12610119 3 C PLIVIT D3 CHOLECALCIFEROL 1 Unknown U 0
126101191 12610119 4 C CALCIUM CALCIUM 1 Unknown UNK U 0
126101191 12610119 5 C POTASSIUM POTASSIUM 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126101191 12610119 1 Chronic leukaemia
126101191 12610119 3 Product used for unknown indication
126101191 12610119 4 Product used for unknown indication
126101191 12610119 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126101191 12610119 HO
126101191 12610119 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126101191 12610119 Anger
126101191 12610119 Dyspnoea
126101191 12610119 Electrocardiogram QT prolonged
126101191 12610119 Hyperhidrosis
126101191 12610119 Myalgia
126101191 12610119 Red blood cell sedimentation rate increased
126101191 12610119 Tremor

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126101191 12610119 2 2014 0